Search results for "Cumene"

showing 10 items of 19 documents

Distribution of betalain pigments in red blood cells after consumption of cactus pear fruits and increased resistance of the cells to ex vivo induced…

2005

Betalain pigments are bioavailable phytochemicals recently acknowledged as natural radical scavengers. This work, which extends previous research on the postabsorbitive fate of dietary betalains, investigated the distribution of betanin and indicaxanthin in red blood cells (RBCs) isolated from healthy volunteers (n = 8), before and during the 1-8 h interval after a cactus pear fruit meal, and the potential antioxidative activity of the pigments in these cells. A peak concentration of indicaxanthin (1.03 +/- 0.2 microM) was observed in RBCs isolated at 3 h after fruit feeding, whereas the concentration at 5 h was about half, and even smaller amounts were measured at 8 h. Indicaxanthin was no…

AdultCactaceaeMaleAntioxidantErythrocytesIndolesPyridinesmedicine.medical_treatmentBetalainsindicaxanthinred blood cellBiologyHemolysischemistry.chemical_compoundBetalainBotanymedicineHumansFood sciencecactus pear; betalains; betanin; indicaxanthin; red blood cell; oxidative hemolysis; bioavailable phytochemicalsBetaninbioavailable phytochemicalsbetaninbetalainGeneral Chemistrymedicine.diseaseHemolysisBetaxanthinsDietQuaternary Ammonium CompoundsRed blood celloxidative hemolysiKineticsmedicine.anatomical_structurechemistryCumene hydroperoxideFruitcactus pearFemaleBetacyaninsGeneral Agricultural and Biological SciencesIndicaxanthinEx vivoJournal of agricultural and food chemistry
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Reaction of melatonin with hemoglobin-derived oxoferryl radicals and inhibition of the hydroperoxide-induced hemoglobin denaturation in red blood cel…

2001

Melatonin has been shown to act as a radical scavenger in various chemical and biological model systems in vitro. Kinetic evidence is now provided showing that melatonin inhibits the irreversible degradation of hemoglobin (Hb), when incubated with red blood cells exposed to the oxidant activity of cumene hydroperoxide (cumOOH). A decrease of heme loss and accumulation of soluble methemoglobin (met-Hb) are explained in terms of the interaction of the indoleamine with perferryl Hb ( . Hb[Fe IV = O]), a highly reactive Hb-derived radical species responsible for the irreversible Hb degradation. A kinetic study, in pure chemical solution, showed that melatonin can effectively reduce the oxoferry…

ChemistryRadicalMethemoglobinMelatoninchemistry.chemical_compoundRed blood cellEndocrinologymedicine.anatomical_structureBiochemistryCumene hydroperoxidemedicineTroloxHemoglobinHemehormones hormone substitutes and hormone antagonistsmedicine.drugJournal of Pineal Research
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Structure-reactivity relationship for aromatics transalkylation and isomerization process with TNU-9, MCM-22 and ZSM-5 zeolites, and their industrial…

2011

[EN] TNU-9 is a medium pore zeolite with a complex tridimensional channel system. Its catalytic properties have been studied in some reactions that involve the BTX fraction, such as benzene and toluene alkylation with methanol, ethanol or isopropanol. These reactions use in practice medium pore zeolites such as ZSM-5 (MFI) or MCM-22 (MWW), and the selectivities obtained with TNU-9 are compared and analyzed from the point of view of the zeolite structure and pore topology, as well as from its possible industrial application. For benzene alkylation to give ethylbenzene (EB), TNU-9 is an active and selective catalyst with selectivities to EB much higher than ZSM-5 and close to those of the ind…

CumeneChemistryProcess Chemistry and TechnologyBTX aromaticsXyleneTNU-9 zeolitePhotochemistryEthylbenzeneTolueneCatalysisCatalysisBenzene alkylationchemistry.chemical_compoundQUIMICA ORGANICAToluene alkylationZSM-5TransalkylationBenzene
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Epoxidation of stilbene using supported gold nanoparticles: cumyl peroxyl radical activation at the gold nanoparticle surface.

2014

The catalytic epoxidation of cis-stilbene using cumene as a solvent in the presence of supported gold nanoparticles (AuNP) yields a mixture of cis and trans-stilbene oxides. EPR and product distribution studies support a new mechanistic proposal where oxygen centred radicals activate the AuNP surface and form active surface oxygen species responsible for the epoxidation products.

CumeneChemistryRadicalMetals and AlloysNanoparticleGeneral ChemistryPhotochemistryCatalysisProduct distribution3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionCatalysisSolventchemistry.chemical_compoundlawColloidal goldMaterials ChemistryCeramics and CompositesElectron paramagnetic resonanceChemical communications (Cambridge, England)
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Influence of Pore-Volume Topology of Zeolite ITQ-7 in Alkylation and Isomerization of Aromatic Compounds

2002

The void structure of zeolite ITQ-7 (ISV structure) is discussed on the basis of catalytic reaction tests. The isomerization and disproportionation of meta-xylene, and the alkylation of benzene or toluene with either ethanol or isopropanol, on the acidic zeolite have been used as model reactions. The dimensions of its three-dimensional system of channels, with pores between 6.1 and 6.3 A and with lower tortuosity than those of beta zeolite, favor higher ratios of isomerization to disproportionation of meta-xylene, and of mono- to dialkylated products and iso- to n-propylbenzene during alkylation of benzene. These effects are enhanced with a partially coked ITQ-7.

CumeneDisproportionationAlkylationEthylbenzeneTolueneCatalysischemistry.chemical_compoundchemistryPolymer chemistryOrganic chemistryPhysical and Theoretical ChemistryBenzeneZeoliteIsomerizationJournal of Catalysis
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The possibilities of using broadleaf cattail seeds (Typha latifolia L.) as super absorbents for removing aromatic hydrocarbons (BTEX) from an aqueous…

2018

Sorption of oil-related products (including mainly the propellants) is the very basic process that counteracts spreading these types of pollution into environment. Plenty of synthetic substances (including the monoaromatic hydrocarbons) are both from the surface and underground waters. The aim of this study was to present the research’s results on the possibilities of using the broadleaf cattail (Typha latifolia L.) seeds as a sorbent of monoaromatic hydrocarbons from an aqueous solution. In order to increase sorptive capacity, the seeds biomass was submitted for the process of mercerizing in diversified time and temperature in water and the NaOH solution. The removal of benzene, toluene, e…

CumeneEnvironmental EngineeringAqueous solutionSorbentsorptionEcological ModelingwatermercerizationSorptionBTEX010501 environmental sciences01 natural sciencesPollutionTolueneEthylbenzeneArticlechemistry.chemical_compoundchemistryEnvironmental chemistrybroadleaf cattail seedsEnvironmental ChemistryBenzene0105 earth and related environmental sciencesWater Science and TechnologyBTEXWater Air and Soil Pollution
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A New Aluminosilicate Molecular Sieve with a System of Pores between Those of ZSM-5 and Beta Zeolite

2011

[EN] A new aluminosilicate zeolite (ITQ-39) has been synthesized. This is an extensively faulted structure with very small domains that makes the structure elucidation very difficult. However, a combination of adsorption spectroscopy and reactivity studies with selected probe molecules suggests that the pore structure of ITQ-39 is related to that of Beta zeolite, with a three-directional channel system with large pores (12-MR), but with an effective pore diameter between those of Beta and ZSM-5, or a three-directional channel system with interconnected large (12-MR) and medium pores (10-MR). The pore topology of ITQ-39 is very attractive for catalysis and shows excellent results for the pre…

CumeneInorganic chemistryGeneral ChemistryMolecular sieveBiochemistryCatalysisCatalysischemistry.chemical_compoundColloid and Surface ChemistryAdsorptionQUIMICA ORGANICAchemistryAluminosilicateReactivity (chemistry)ZSM-5Zeolite
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Thermal frontal polymerization with a thermally released redox catalyst

2012

ABSTRACT: We studied thermal frontal polymerization using a re-dox systeminan attempt to lower the temperature of thefrontallypolymerizable system while increasing the front velocity so as toobtain a self-sustaining front in a thinner layer than without theredox components. A cobalt-containing polymer with a meltingpoint of 63 C (Intelimer 6050X11) and cumene hydroperoxidewere used with a triacrylate. The use of the Intelimer decreasedthe front velocity but allowed fronts to propagate in thinner layersand with more filler while still having a pot life of days. Nonplanarmodes of propagation occurred. Fronts propagated faster when6-O-palmitoyl- L -ascorbic acid was used as a reductant. Intere…

CumeneMaterials sciencePolymers and PlasticsRadical polymerizationkineticfrontal polymerizationchemistry.chemical_compoundPolymer chemistryMaterials ChemistryFront velocityredox polymersSettore CHIM/02 - Chimica Fisicaaddition polymerizationchemistry.chemical_classificationAcrylateOrganic ChemistryacrylatePolymeracrylate; addition polymerization; frontal polymerization; kinetics; radical polymerization; redox polymersAscorbic acidradical polymerizationchemistryPolymerizationChemical engineeringAddition polymerJournal of Polymer Science Part A: Polymer Chemistry
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Insights into the Mechanism of Cumene Peroxidation Using Supported Gold and Silver Nanoparticles

2013

Due to the considerable industrial implications, an in-depth study of cumene peroxidation using supported gold and silver nanoparticles was carried out to gain more insight into the mechanism of this reaction. Supported gold nanoparticles were found to efficiently catalyze the decomposition of cumene hydroperoxide with a selectivity of 25% at 80 °C when using gold supported on hydrotalcite (AuNP@HT), and 2-phenyl-2-propanol (i.e., cumyl alcohol) was the main product. Further, silver nanoparticles supported on hydrotalcite (AgNP@HT) converted cumene to cumene hydroperoxide at 80 °C with 80% selectivity. Both benchtop and oxygen-uptake experiments were used to probe the reaction mechanism and…

CumeneReaction mechanismHydrotalcite010405 organic chemistryChemistryGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesCatalysisSilver nanoparticle0104 chemical sciences3. Good healthCatalysischemistry.chemical_compoundCumene hydroperoxideColloidal goldSelectivityACS Catalysis
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Nachweis des di-2-cyanoisopropylperoxides bei der zersetzung von azoisobuttersäuredinitril in gegenwart von sauerstoff

1970

Das Di-2-cyanoisopropylperoxid entsteht in etwa 5-proz. Ausbeute bei der Zersetzung von Azoisobuttersaredinitril unter Sauerstoff in Isobutyronitril als Losungsmittel. Thermisch zerfallt das Peroxid est oberhalb von 120°C mit mesbarer Geschwindigkeit in einer Reaktion erster Ordnung. Die Aktivierungsenergie, in Cumol als Losungsmittel, wurde zu 37,9 kcal · mol−1 bestimmt. Werte fur die Zerfallskonstante bei 140°C sind in Cumol 0,057 h−1, in tert-Butylbenzol 0,073 h−1, in Chlorbenzol 0,18 h−1 und in o-Dichlorbenzol 0,23 h−1. Di-2-cyanoisopropylperoxide is formed when azobisisobutyronitrile is decomposed under oxygen in isobutyronitrile as a solvent. The yield amounts to ca. 5%. Thermal decom…

CumeneSolventchemistry.chemical_compoundReaction rate constantchemistryChlorobenzenePolymer chemistryThermal decompositionAzobisisobutyronitrilePeroxideChemical decompositionDie Makromolekulare Chemie
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